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Quality Control in Clinical Trials Blinding, Clinical ... - summitMD.com

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• Manag<strong>in</strong>g data<br />

Bl<strong>in</strong>d<strong>in</strong>g<br />

• Limit access to data<br />

• Develop list of assigned personnel and their roles<br />

• Limit pr<strong>in</strong>t<strong>in</strong>g of data <strong>in</strong>clud<strong>in</strong>g where to pr<strong>in</strong>t<br />

• Shred pr<strong>in</strong>ted items unless required for<br />

recordkeep<strong>in</strong>g<br />

• do not place <strong>in</strong> trash (too easy for others to pick up and<br />

read)<br />

• Provide isolated area for data review, analysis, data<br />

entry, source document collection for safety<br />

monitor<strong>in</strong>g<br />

• Use <strong>com</strong>puter screen shades when work<strong>in</strong>g <strong>in</strong> open<br />

areas

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